Anar al contingut
VuFind
English
Deutsch
Español
Français
Italiano
日本語
Nederlands
Português
Português (Brasil)
中文(简体)
中文(繁體)
Türkçe
עברית
Gaeilge
Cymraeg
Ελληνικά
Català
Euskara
Русский
Čeština
Suomi
Svenska
polski
Dansk
slovenščina
اللغة العربية
বাংলা
Galego
Tiếng Việt
Hrvatski
हिंदी
Հայերէն
Українська
Sámegiella
Монгол
Idioma
Tots els camps
Títol
Autor
Matèria
Signatura
ISBN/ISSN
Etiqueta
Trobar
Avançada
Identification and functional...
Citar
Enviar aquest missatge de text
Enviar per correu electrònic aquest
Imprimir
Exportar registre
Exportar a RefWorks
Exportar a EndNoteWeb
Exportar a EndNote
Enllaç permanent
Identification and functional analysis of cardiac troponin I as a novel disease gene in autosomal dominant familial dilated cardiomyopathy
Dades bibliogràfiques
Autors principals:
Carballo, S
,
Redwood, C
,
Robinson, P
,
Blair, E
,
Watkins, H
Format:
Conference item
Publicat:
2006
Fons
Descripció
Ítems similars
Visualització del personal
Ítems similars
Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy.
per: Carballo, S, et al.
Publicat: (2009)
Autosomal dominant familial dilated cardiomyopathy caused by a novel mutation in phospholamban
per: Carballo, S, et al.
Publicat: (2004)
A novel mutation in phospholamban causes a mixed hypertrophic and dilated cardiomyopathy phenotype with autosomal dominant inheritance
per: Carballo, S, et al.
Publicat: (2004)
Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
per: Robinson, P, et al.
Publicat: (2007)
Functional effects of mutations in troponin T and tropomyosin which cause dilated cardiomyopathy
per: Robinson, P, et al.
Publicat: (2003)